Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930407I10Rik |
A |
T |
15: 81,950,622 (GRCm39) |
R1506S |
probably benign |
Het |
Acox2 |
T |
C |
14: 8,247,960 (GRCm38) |
T441A |
probably damaging |
Het |
Adam6a |
A |
G |
12: 113,508,917 (GRCm39) |
E430G |
probably damaging |
Het |
Afg3l2 |
T |
C |
18: 67,540,439 (GRCm39) |
E690G |
probably damaging |
Het |
Alb |
A |
G |
5: 90,611,873 (GRCm39) |
I101V |
probably benign |
Het |
Arhgef19 |
T |
C |
4: 140,976,903 (GRCm39) |
I493T |
possibly damaging |
Het |
Btnl2 |
T |
C |
17: 34,577,028 (GRCm39) |
M61T |
probably benign |
Het |
Cyp2d11 |
A |
G |
15: 82,273,429 (GRCm39) |
Y481H |
probably benign |
Het |
Dennd4c |
T |
C |
4: 86,744,319 (GRCm39) |
|
probably null |
Het |
Dhx9 |
C |
A |
1: 153,334,182 (GRCm39) |
V993F |
possibly damaging |
Het |
Dlk1 |
A |
G |
12: 109,424,066 (GRCm39) |
Q110R |
probably null |
Het |
Dmp1 |
A |
C |
5: 104,360,269 (GRCm39) |
D315A |
probably damaging |
Het |
Dnah3 |
T |
C |
7: 119,550,591 (GRCm39) |
K3243E |
probably damaging |
Het |
Dsc3 |
T |
C |
18: 20,101,449 (GRCm39) |
N648S |
probably benign |
Het |
Dsc3 |
C |
T |
18: 20,114,274 (GRCm39) |
D327N |
probably damaging |
Het |
Egr4 |
T |
C |
6: 85,489,106 (GRCm39) |
D318G |
probably damaging |
Het |
Fiz1 |
A |
T |
7: 5,012,163 (GRCm39) |
C118* |
probably null |
Het |
Flad1 |
A |
C |
3: 89,310,517 (GRCm39) |
Y479D |
probably damaging |
Het |
Flnb |
T |
C |
14: 7,929,939 (GRCm38) |
F2023S |
probably damaging |
Het |
Glp1r |
T |
C |
17: 31,143,531 (GRCm39) |
L189P |
probably damaging |
Het |
Grm5 |
A |
T |
7: 87,779,724 (GRCm39) |
T1055S |
probably benign |
Het |
Gucy1a1 |
A |
G |
3: 82,018,468 (GRCm39) |
I123T |
probably benign |
Het |
Ifnar1 |
T |
A |
16: 91,292,344 (GRCm39) |
C199* |
probably null |
Het |
Lepr |
A |
T |
4: 101,622,612 (GRCm39) |
Y464F |
probably damaging |
Het |
Mamdc4 |
G |
T |
2: 25,457,730 (GRCm39) |
Q452K |
possibly damaging |
Het |
Map2k6 |
A |
G |
11: 110,290,175 (GRCm39) |
|
probably benign |
Het |
Mphosph10 |
T |
C |
7: 64,034,076 (GRCm39) |
I429V |
possibly damaging |
Het |
Neb |
T |
A |
2: 52,181,074 (GRCm39) |
M1178L |
possibly damaging |
Het |
Nherf4 |
T |
C |
9: 44,159,670 (GRCm39) |
E442G |
probably damaging |
Het |
Npc2 |
C |
A |
12: 84,807,612 (GRCm39) |
R82L |
probably benign |
Het |
Olfm5 |
A |
T |
7: 103,803,029 (GRCm39) |
M478K |
probably benign |
Het |
Or5aq6 |
G |
T |
2: 86,923,670 (GRCm39) |
Q24K |
probably benign |
Het |
Or5k14 |
A |
C |
16: 58,693,016 (GRCm39) |
L166V |
probably damaging |
Het |
Osbpl9 |
T |
C |
4: 109,013,908 (GRCm39) |
D62G |
probably damaging |
Het |
Otog |
C |
T |
7: 45,901,473 (GRCm39) |
R391C |
probably damaging |
Het |
Plppr4 |
T |
C |
3: 117,115,592 (GRCm39) |
Y755C |
probably damaging |
Het |
Pnpla8 |
T |
A |
12: 44,358,368 (GRCm39) |
F708I |
possibly damaging |
Het |
Pom121l12 |
A |
T |
11: 14,549,932 (GRCm39) |
T213S |
probably benign |
Het |
Pramel27 |
T |
A |
4: 143,579,601 (GRCm39) |
D395E |
probably benign |
Het |
Rabep1 |
T |
C |
11: 70,799,332 (GRCm39) |
S278P |
probably benign |
Het |
Rigi |
A |
G |
4: 40,225,596 (GRCm39) |
|
probably null |
Het |
Rnf213 |
C |
G |
11: 119,365,031 (GRCm39) |
Q4563E |
probably benign |
Het |
Rttn |
C |
A |
18: 89,131,467 (GRCm39) |
R1949S |
probably benign |
Het |
Rwdd3 |
T |
C |
3: 120,952,788 (GRCm39) |
I140V |
probably benign |
Het |
Serpinb6a |
A |
T |
13: 34,115,462 (GRCm39) |
M53K |
probably damaging |
Het |
Serpinb9g |
A |
T |
13: 33,676,896 (GRCm39) |
D226V |
possibly damaging |
Het |
Serpind1 |
A |
T |
16: 17,160,847 (GRCm39) |
Y459F |
probably damaging |
Het |
Skor2 |
T |
C |
18: 76,946,569 (GRCm39) |
V97A |
unknown |
Het |
Slc26a4 |
C |
T |
12: 31,599,911 (GRCm39) |
|
probably null |
Het |
Slc4a10 |
T |
C |
2: 62,097,851 (GRCm39) |
Y517H |
probably damaging |
Het |
Sphkap |
A |
G |
1: 83,254,909 (GRCm39) |
W947R |
probably damaging |
Het |
Sult3a2 |
T |
C |
10: 33,653,239 (GRCm39) |
D167G |
probably damaging |
Het |
Supt16 |
A |
T |
14: 52,410,020 (GRCm39) |
M729K |
probably damaging |
Het |
Tmem176b |
A |
G |
6: 48,811,538 (GRCm39) |
I37T |
possibly damaging |
Het |
Tmem259 |
A |
G |
10: 79,813,819 (GRCm39) |
V423A |
probably damaging |
Het |
Tmem62 |
G |
T |
2: 120,837,533 (GRCm39) |
L483F |
probably damaging |
Het |
Tnfrsf13b |
T |
C |
11: 61,031,777 (GRCm39) |
|
probably null |
Het |
Tut7 |
A |
T |
13: 59,937,074 (GRCm39) |
I1191K |
probably damaging |
Het |
Ube2w |
A |
C |
1: 16,672,542 (GRCm39) |
N46K |
probably benign |
Het |
Unc79 |
A |
T |
12: 103,013,922 (GRCm39) |
H300L |
probably damaging |
Het |
Unc79 |
T |
A |
12: 103,049,855 (GRCm39) |
H920Q |
probably benign |
Het |
Vmn1r16 |
A |
G |
6: 57,299,900 (GRCm39) |
Y241H |
probably damaging |
Het |
Vmn2r100 |
A |
T |
17: 19,742,459 (GRCm39) |
I278F |
possibly damaging |
Het |
Zfp260 |
T |
A |
7: 29,804,884 (GRCm39) |
H261Q |
probably damaging |
Het |
|
Other mutations in Txk |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02337:Txk
|
APN |
5 |
72,864,889 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02602:Txk
|
APN |
5 |
72,865,063 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03353:Txk
|
APN |
5 |
72,893,745 (GRCm39) |
missense |
probably benign |
|
BB007:Txk
|
UTSW |
5 |
72,892,536 (GRCm39) |
missense |
probably damaging |
1.00 |
BB017:Txk
|
UTSW |
5 |
72,892,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R0402:Txk
|
UTSW |
5 |
72,889,105 (GRCm39) |
critical splice donor site |
probably null |
|
R1509:Txk
|
UTSW |
5 |
72,856,453 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Txk
|
UTSW |
5 |
72,865,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R2913:Txk
|
UTSW |
5 |
72,881,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R2914:Txk
|
UTSW |
5 |
72,881,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R3722:Txk
|
UTSW |
5 |
72,865,078 (GRCm39) |
nonsense |
probably null |
|
R4080:Txk
|
UTSW |
5 |
72,858,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R5341:Txk
|
UTSW |
5 |
72,853,964 (GRCm39) |
missense |
probably benign |
0.08 |
R5580:Txk
|
UTSW |
5 |
72,864,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R6155:Txk
|
UTSW |
5 |
72,858,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R6310:Txk
|
UTSW |
5 |
72,893,760 (GRCm39) |
missense |
probably benign |
0.01 |
R6382:Txk
|
UTSW |
5 |
72,893,823 (GRCm39) |
intron |
probably benign |
|
R6938:Txk
|
UTSW |
5 |
72,856,492 (GRCm39) |
missense |
probably damaging |
0.99 |
R7225:Txk
|
UTSW |
5 |
72,858,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R7327:Txk
|
UTSW |
5 |
72,873,226 (GRCm39) |
missense |
probably damaging |
0.98 |
R7337:Txk
|
UTSW |
5 |
72,889,109 (GRCm39) |
nonsense |
probably null |
|
R7436:Txk
|
UTSW |
5 |
72,853,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Txk
|
UTSW |
5 |
72,893,726 (GRCm39) |
missense |
unknown |
|
R7709:Txk
|
UTSW |
5 |
72,864,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R7725:Txk
|
UTSW |
5 |
72,864,900 (GRCm39) |
missense |
probably damaging |
0.96 |
R7930:Txk
|
UTSW |
5 |
72,892,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R8124:Txk
|
UTSW |
5 |
72,860,606 (GRCm39) |
splice site |
probably null |
|
R8754:Txk
|
UTSW |
5 |
72,889,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8901:Txk
|
UTSW |
5 |
72,858,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R9245:Txk
|
UTSW |
5 |
72,891,610 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Txk
|
UTSW |
5 |
72,892,554 (GRCm39) |
missense |
unknown |
|
|